Characterization of functional domains of the SMN protein in vivo (Q40778498)

23 September 2017

title

Characterization of functional domains of the SMN protein in vivo (English)

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23 September 2017

Wang J

1

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23 September 2017

Dreyfuss G

series ordinal

2

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23 September 2017

language of work or name

English

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publication date

25 September 2001

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Journal of Biological Chemistry

23 September 2017

published in

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23 September 2017

volume

276

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23 September 2017

issue

48

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23 September 2017

page(s)

45387-45393

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The genetic component in child mortality

23 September 2017

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Characterization of the Schizosaccharomyces pombe orthologue of the human survival motor neuron (SMN) protein

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The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

21 January 2018

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Identification of survival motor neuron as a transcriptional activator-binding protein.

21 January 2018

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The survival motor neuron protein interacts with the transactivator FUSE binding protein from human fetal brain

21 January 2018

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Specific sequences of the Sm and Sm-like (Lsm) proteins mediate their interaction with the spinal muscular atrophy disease gene product (SMN).

21 January 2018

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Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli

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Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?

21 January 2018

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The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

21 January 2018

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A cell system with targeted disruption of the SMN gene: functional conservation of the SMN protein and dependence of Gemin2 on SMN.

21 January 2018

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The Schizosaccharomyces pombe protein Yab8p and a novel factor, Yip1p, share structural and functional similarity with the spinal muscular atrophy-associated proteins SMN and SIP1.

21 January 2018

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SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.

21 January 2018

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Tudor domains in proteins that interact with RNA.

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Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs

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Characterization of a gene encoding survival motor neuron (SMN)-related protein, a constituent of the spliceosome complex

21 January 2018

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SMN tudor domain structure and its interaction with the Sm proteins

21 January 2018

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Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy

21 January 2018

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A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing

21 January 2018

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A functional interaction between the survival motor neuron complex and RNA polymerase II

21 January 2018

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Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

21 January 2018

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21 January 2018

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The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy

21 January 2018

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Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy

21 January 2018

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Deletion of murine SMN exon 7 directed to skeletal muscle leads to severe muscular dystrophy

21 January 2018

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The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding.

21 January 2018

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The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding

21 January 2018

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Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals

21 January 2018

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The survival motor neuron protein of Schizosacharomyces pombe. Conservation of survival motor neuron interaction domains in divergent organisms

21 January 2018

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A role for polyproline motifs in the spinal muscular atrophy protein SMN. Profilins bind to and colocalize with smn in nuclear gems

21 January 2018

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SMN oligomerization defect correlates with spinal muscular atrophy severity

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M105059200

1 reference

23 September 2017

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